词条 | Embryo rescue |
释义 |
HistoryEmbryo rescue was first documented in the 18th century when Charles Bonnet excised Phaseolus and Fagopyrum embryos and was successful in it , planted them in soil and the cross resulted in dwarf plants.[5] Soon after this, scientists began placing the embryos in various nutrient media. During the period of 1890 to 1904, systems for embryo rescue became systematic by applying nutrient solutions that contained salts and sugars and applying aseptic technique.[6] The first successful in vitro embryo culture was performed by Hanning in 1904, he however described problems with precocious embryos that resulted in small, weak, and often inviable plantlets.[7] Applications
TechniquesDepending on the organ cultured, it may be referred to as either embryo, ovule, or ovary culture. Ovule culture or in ovolo embryo culture is a modified technique of embryo rescue whereby embryos are cultured while still inside their ovules to prevent damaging them during the excision process.[8] Ovary or pod culture, on the other hand employs the use of an entire ovary into culture. It becomes necessary to excise the entire small embryo to prevent early embryo abortion. However, it is technically difficult to isolate the tiny intact embryos, so often ovaries with young embryos, or entire fertilized ovules will be used.[9] Factors to considerEmbryos are manually excised and placed immediately onto a culture medium that provides the proper nutrients to support survival and growth (Miyajima 2006). While the disinfestation and explant excision processes differ for these three techniques, many of the factors that contribute to the successful recovery of viable plants are similar. The main factors that influence success are; the time of culture, the composition of the medium, and temperature and light. Timing mainly refers to the maturation stage of the embryo before excision. The optimal time especially for the rescue of embryos involving incompatible crosses would be just prior to embryo abortion. Nevertheless, due to difficulties involved with the rearing of young embryos compared to those that have reached the autotrophic phase of development, embryos are normally allowed to develop in vivo as long as possible. While in general, two main types of basal media are the most commonly used for embryo rescue studies, i.e. Murashige and Skoog medium (MS) [10] and Gamborg’s B-5[11] media (Bridgen, 1994), the composition of the medium will vary in terms of the concentrations of media supplements required. This will generally depend on the stage of development of the embryo. For instance, young embryos would require a complex medium with high sucrose concentrations, while more mature embryos can usually develop on a simple medium with low levels of sucrose. The temperature and light requirement is generally species specific and thus its usually regulated to be the within the same temperature requirement as that of its parent with embryos of cool-season crops requiring lower temperatures than those of warm-season crops. Both plant and animal cells, tissues and organ culture is possible in artificial nutrient medium in controlled laboratory conditions. Many desired products can be obtained through tissue culture like pharmaceutical drugs, vaccines, monoclonal antibodies. See also
References1. ^{{cite journal|last=Sage|first=T.L.|author2=Strumas, F. |author3=Cole, W.W. |author4=Barret,S |title=Embryo rescue and plant regeneration following interspecific crosses in the genus Hylocereus (Cactaceae)|journal=Euphytica|year=2010|volume=174|pages=73–82|doi=10.1007/s10681-010-0135-x}} 2. ^{{cite journal|last=Miyajuma|first=D.|title=Ovules that failed to form seeds in zinnia (Zinnia violacec Cav)|journal=Sci Hortic|year=2006|volume=107|pages=176–182|doi=10.1016/j.scienta.2005.06.014|issue=2}} 3. ^{{cite book|last=Reed|first=Sandra|title=Plant Development and Biotechnology|year=2005|publisher=CRC Press|isbn=0-8493-1614-6|pages=235–239|url=http://ddr.nal.usda.gov/bitstream/10113/42085/1/IND44376954.pdf|editor=Robert N. Trigiano|editor2=Dennis J. Gray}} 4. ^{{cite journal|last=Bridgen|first=Mark P.|title=A Review of Plant Embryo Culture|journal=HortScience|year=1994|volume= 29|pages=1243–1246}} 5. ^{{cite journal|last=Sharma|first=D.R. |author2=Daur, R. |author3=Kumar K.|title=Embryo rescue in plants-a review|journal=Euphytica|year=1996|volume=89|pages=325–337|doi=10.1007/BF00022289}} 6. ^{{cite journal|last=Amanate-Bordeos|first=A.D. |author2=Nelson, R.J. |author3=Oliva, N.P. |author4=Dalmacio, R.D. |author5=Leung, H. |author6=Sitch, L.A.|title=Transfer of blast and bacterial blight resistance from the tetrapliod wild rice Oryza minuta to the cultivated rice, O. sativa|journal=Theor. Appl. Genet.|year=1992|volume=84|pages=345–354 |doi=10.1007/bf00229493}} 7. ^{{cite journal|last=Mehetre|first=S. S|author2=Aher, A. R.|title=Embryo rescue: A tool to overcome incompatible interspecific hybridization in Gossypium Linn. --A review|journal=Indian Journal of Biotechnology|year=2004|volume=3|pages=29–36}} 8. ^{{cite journal|last=Cisneros|first=Aroldo|author2=Tel-Zur|title=Embryo rescue and plant regeneration following interspecific crosses in the genus Hylocereus (Cactaceae)|journal=Euphytica|year=2010|volume=174|pages=73–82|doi=10.1007/s10681-010-0135-x}} 9. ^{{cite journal|last=Ikeda|first=N.|author2=Niimi, Y. Han D.|title=Production of seedling from ovules excised at the zygote stage in Lilium spp|journal=Plant Cell Tissue Organ Cult|year=2003|volume=73|pages=159–166|doi=10.1023/A:1022818413617|issue=2}} 10. ^{{cite journal|last=Murashige|first=T|author2=Skoog, F.|title=A revised medium for rapid growth and bioassays with tobacco tissue cultures|journal=Physiol. Plant.|year=1962|volume=15|pages=473–497|doi=10.1111/j.1399-3054.1962.tb08052.x|issue=3}} 11. ^{{cite journal|last=Gamborg|first=O.L |author2=Miller, R.A. |author3=Ojima, K.|title=Nutrient requirements of suspension cultures of soybean root cells|journal=Exp. Cell Res.|year=1968|volume=50|issue=1|pages=151–158 [157] | doi = 10.1016/0014-4827(68)90403-5 | pmid=5650857}} External links
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